Job Description
Job Description
We are seeking a full-time Clinical Research Coordinator (CRC) to support a variety of human subject research studies. This position provides a unique opportunity to work alongside experienced investigators, research coordinators, and clinicians engaged in clinical trials targeting memory disorders, neurodegenerative diseases, brain injury, and environmentally linked health conditions. This is an excellent opportunity for recent graduates or early-career professionals interested in neuroscience, psychology, public health, or clinical research. Training will be provided, and there is strong potential for professional growth and advancement within the Institute’s research programs. The Roskamp Institute Clinic is seeking a full-time Clinical Research Coordinator Assistant to work with our Clinical Trials Department staff. The ideal candidate will be eager to learn about and perform tasks associated with clinical trial protocols for subjects with neuro-degenerative diseases.
The ideal candidate must be willing to do a variety of interesting and challenging tasks including:
• Preparing clinical research study protocols, consent forms and electronic data capture documents.
• using Microsoft Word to prepare detailed source forms to record trial patient visit data
• entering source form data into several electronic data systems from individual trial sponsors
• working with trial coordinators to respond to questions and resolve queries from trial sponsors about the data that was entered into the systems
• organizing and keeping track of an inventory medical supply kits, re-ordering as needed and disposing of expired items
• downloading, printing and filing the temperature logs for refrigerated supplies and emailing the logs to the sponsors' trial monitors
• entering trial patient and visit data into Roskamp Institute's online clinical trial patient and visit tracking and accounting system
• searching the Roskamp Clinic's Electronic Medical Records database to identify patients who might be suitable candidates for clinical trials
• reading patient medical records to determine whether they meet the criteria to participate in clinical trials
• recruiting and screening patients for clinical trials by calling them to explain the clinical trial protocol, responding to their questions, and obtaining information to determine if the patient would meet the clinical trial participation criteria
• scheduling clinical trial visit appointments and calling patients to remind them of upcoming appointments
• responding to phone calls and scheduling appointments for people seeking memory screening tests
• learning how to design, set up, enter data and produce reports from an online database that specializes in in-house research studies.
This challenging position would appeal to a candidate with these skills and work practices:
• able to communicate clearly with people in a patient, respectful, considerate and empathetic manner by phone and email
• extremely well organized, careful, thorough and detail oriented
• comfortable with learning how to use several computer applications to enter data and schedule appointments
• able to read and understand medical terminology
• willing to assist two or more clinical trial coordinators and perform tasks as requested
• able to multi-task, work diligently and manage work priorities
• even-tempered and congenial manner
• willing to learn and absorb new information on an ongoing basis
Job Type: Full-time
Salary - $19 to $22 per hour, based on previous experience.
Full time staff are eligible to receive insurance and additional benefits, including health, dental, vision, 401(k), etc.
Please upload your resume and include a brief cover letter describing your interest in this role and relevant experience.
Application Questions
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- When are you available for an interview or phone screen? Please list 2-3 dates and times or ranges of times.
Typical work schedule is from 9 AM to 5 PM Monday to Friday. 40 hour work week.